Fsihi H, Vincent V, Cole S T
Unite de Genetique Moleculaire Bacterienne, Institut Pasteur, Paris, France.
Proc Natl Acad Sci U S A. 1996 Apr 16;93(8):3410-5. doi: 10.1073/pnas.93.8.3410.
The A subunit of DNA gyrase in Mycobacterium leprae, unlike its counterpart in Mycobacterium tuberculosis, is produced by protein splicing as its gene, gyrA, harbors a 1260-bp in-frame insertion encoding an intein, a putative homing endonuclease. Analysis of the gyrA locus from different mycobacterial species revealed the presence of inteins in Mycobacterium flavescens, Mycobacterium gordonae and Mycobacterium kansasii but not in 10 other pathogenic or saprophytic mycobacteria. In all four cases where intein coding sequences were found, they were localized in the same position in gyrA, immediately downstream of the codon for the key active-site residue Tyr-130. The intein products were similar, but not identical, in sequence and the splice junctions displayed all the features found in other polypeptides known to be produced by protein splicing from a precursor protein. Paired motifs, found in homing endonucleases encoded by some group I RNA introns, and inteins showing endonuclease activity, were present in the gyrA inteins as were other intein-specific signatures. Some strains of M. flavescens, M. gordonae, and M. kansasii were shown by PCR analysis to have inteinless gyrA genes, in contrast to the situation in M. leprae where all the isolates possessed insertions in gyrA. Sequencing of the corresponding regions revealed that, although the GyrA protein sequence was conserved, the nucleotide sequences differed in gyrA genes with and without inteins, suggesting that the homing endonuclease displays sequence specificity.
麻风分枝杆菌中的DNA促旋酶A亚基,与其在结核分枝杆菌中的对应亚基不同,是通过蛋白质剪接产生的,因为其基因gyrA含有一个1260 bp的框内插入序列,该序列编码一个内含肽,一种假定的归巢内切核酸酶。对不同分枝杆菌物种的gyrA基因座进行分析发现,微黄分枝杆菌、戈登分枝杆菌和堪萨斯分枝杆菌中存在内含肽,但在其他10种致病性或腐生性分枝杆菌中不存在。在所有发现内含肽编码序列的4个案例中,它们都位于gyrA的同一位置,紧挨着关键活性位点残基Tyr-130的密码子下游。内含肽产物在序列上相似但不相同,剪接位点呈现出已知由前体蛋白通过蛋白质剪接产生的其他多肽中发现的所有特征。在一些I类RNA内含子编码的归巢内切核酸酶中发现的配对基序,以及显示内切核酸酶活性的内含肽,在gyrA内含肽中也存在,其他内含肽特异性特征也是如此。通过PCR分析表明,一些微黄分枝杆菌、戈登分枝杆菌和堪萨斯分枝杆菌菌株具有无内含肽的gyrA基因,这与麻风分枝杆菌的情况形成对比,在麻风分枝杆菌中,所有分离株的gyrA都有插入序列。相应区域的测序表明,尽管GyrA蛋白序列保守,但有内含肽和无内含肽的gyrA基因的核苷酸序列不同,这表明归巢内切核酸酶具有序列特异性。